Sun Pack S.A.S
FDA import alert and refusal historyBogota, ColombiaFEI 3023058393
Recorded by FDA as SUN PACK S.A.S
As of October 26, 2026, Sun Pack S.A.S (Bogota, Colombia) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for limes, published by FDA on October 11, 2022, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-05 · red list
- Last import refusal
- Lime (citrus) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Sun Pack S.A.S
2 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 99-05red listLimesSource
- Import refusalRefused, Lime (citrus)PESTICIDEEntry 9P3-0256743-9Source
Refusal charges, in plain English
- PESTICIDE1 refused line
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about Sun Pack S.A.S
- Is Sun Pack S.A.S on an FDA import alert?
- Yes. As of October 26, 2026, Sun Pack S.A.S is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for limes; FDA published the listing on October 11, 2022.
- Has FDA refused shipments from Sun Pack S.A.S?
- Yes. FDA refused 1 shipment line from Sun Pack S.A.S on September 29, 2022. The most recent, on September 29, 2022, was lime (citrus), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Sun Pack S.A.S's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Sun Pack S.A.S's FEI number?
- Sun Pack S.A.S's FDA Establishment Identifier (FEI) is 3023058393.
- Can shipments from Sun Pack S.A.S still enter the U.S.?
- Shipments of limes from Sun Pack S.A.S can be detained without physical examination under Import Alert 99-05; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.